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Items: 10

1.

Individual and family characteristics associated with protein truncating BRCA1 and BRCA2 mutations in an Ontario population based series from the Cooperative Family Registry for Breast Cancer Studies.

Ozcelik H, Knight JA, Glendon G, Yazici H, Carson N, Ainsworth PJ, Taylor SA, Feilotter H, Carter RF, Boyd NF, Andrulis IL; Ontario Cancer Genetics Network.

J Med Genet. 2003 Aug;40(8):e91. No abstract available.

2.

Management updates for women with a BRCA1 or BRCA2 mutation.

Nusbaum R, Isaacs C.

Mol Diagn Ther. 2007;11(3):133-44. Review.

PMID:
17570734
4.

BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk families.

Sinilnikova OM, Mazoyer S, Bonnardel C, Lynch HT, Narod SA, Lenoir GM.

Fam Cancer. 2006;5(1):15-20. Review.

PMID:
16528604
5.

[Candidate genes for the familial forms of breast and ovarian carcinomas (BRCA)].

Markov A.

Mol Med (Sofia). 1996;1(1):17-20. Review. Bulgarian. No abstract available.

PMID:
8974760
6.

[Prospects for genetic diagnosis].

Shimoji T, Miki Y.

Nihon Rinsho. 2007 Jun 28;65 Suppl 6:241-4. Review. Japanese. No abstract available.

PMID:
17682161
7.

BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.

Tammaro C, Raponi M, Wilson DI, Baralle D.

Biochem Soc Trans. 2012 Aug;40(4):768-72. doi: 10.1042/BST20120140. Review.

PMID:
22817731
8.

Breast cancer in Morocco: a literature review.

Slaoui M, Razine R, Ibrahimi A, Attaleb M, Mzibri ME, Amrani M.

Asian Pac J Cancer Prev. 2014;15(3):1067-74. Review.

9.

Participation in the cooperative family registry for breast cancer studies: issues of informed consent.

Daly MB, Offit K, Li F, Glendon G, Yaker A, West D, Koenig B, McCredie M, Venne V, Nayfield S, Seminara D.

J Natl Cancer Inst. 2000 Mar 15;92(6):452-6. Review. No abstract available.

10.

The impact of genetic developments on breast cancer.

Favors AC Jr.

Med Sect Proc. 1995:49-59. Review. No abstract available.

PMID:
8677252
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